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Wyeth received an FDA warning letter in May 2006 that raised several specific concerns about manufacturing at the facility. Based on the nature of the inspection observations issued

According to the trial protocol, enrollment of subjects of the main cohort may be initiated only if a limited number subjects of the first cohort experience adverse events.

This new animal data demonstrate that oral administration of Guanilib significantly reduces gastrointestinal (GI) inflammation, and confirm earlier evidence of down-regulation of interleukin-17 (IL-17), IL-23, and tumor necrosis

Pegintron is administered once weekly at an individualized dose according to a patient’s weight and is the only pegylated interferon indicated in China for a 24 week treatment

The E1.7 million grant which was awarded to a consortium of nine leading universities and companies working in the field of influenza research, will finance preclinical and clinical

The study examined the effects of the Tibotec’s protease-inhibitor Prezista (darunavir), when combined with a low dose of the current antiretroviral ritonavir. The researchers checked for levels of

Adventrx is conducting preclinical pharmacokinetic testing of the drug, ANX-514, to compare this product candidate with the approved version of the product, marketed under the brand name Taxotere.

Previous studies have suggested that ibuprofen interferes with the effects of aspirin. In the study patients were taking either high dose, 400mg a day lumiracoxib, a type of

The study aims to demonstrate the dose, safety and immunogenicity of Intercell’s JE vaccine compared to a locally produced mouse-brain Japanese encephalitis vaccine. It is the first step